There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, and friends who struggle every day just to breathe. I walk for them. I especially walk for a very special girl, Lisa. She gained her wings 10 years ago at the young age of 25. I made the promise to her I will always help with the fundraising. There has been so much progress made but so much more needs to be done. I have witnessed the improved quality of life for people by new medications and new treatments. The money we raise does make a difference. Will you join me and support my fundraising goal?
Real progress has been made for those who have CF, but there is still no cure for this devastating disease and many lives are cut far too short. We’ve come so far, but there’s still so much work to do. I will not stop striding until all those with cystic fibrosis have a cure. We will not leave anyone behind.
Please support me!
We are at a pivotal moment in the history of cystic fibrosis and your support matters. With your help, we can invest our resources in research today, while raising funds for tomorrow, to ensure we have what it takes to reach the finish line. Together, we can make CF stand for Cure Found. Please help me reach my fundraising goal!
The above is always my go to for fundraising for CF Foundation. If you know me at all you know this is very near and dear to my heart. There's not a day that goes by that I do not miss this girl as well as admire her. I try to keep up with the advances being made and do see first hand that your donation will definitely improve someone's life. There are people I know personally and there are people I am able to keep up with via Facebook. Although they still struggle and suffer their quality of life has improved and to witness that is simply amazing.
So please, take the time and donate!!
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.